Neoadjuvant low-dose radiotherapy with chemoimmunotherapy for advanced head and neck cancer
Neoadjuvant Low-dose Radiotherapy, Tislelizumab, Combined With Albumin-bound Paclitaxel and Cisplatin in Resectable Locally Advanced Head and Neck Squamous Cell Carcinoma (NeoRTPC02): an Open Label, Single-arm, Phase II Clinical Trial
This study is testing a new treatment that combines low-dose radiation with chemotherapy and immunotherapy to see if it helps people with advanced head and neck cancer before surgery.
Quick facts
| Phase | Phase 2 |
|---|---|
| Study type | Interventional |
| Enrollment | 25 (estimated) |
| Ages | 18 Years to 70 Years |
| Sex | All |
| Sponsor | Fifth Affiliated Hospital, Sun Yat-Sen University Academic / other |
| Drugs / interventions | prednisone, tislelizumab |
| Locations | 2 sites (Zhuhai, Guangdong and 1 other locations) |
| Trial ID | NCT05343325 on ClinicalTrials.gov |
What this trial studies
This clinical trial investigates the efficacy and safety of a novel treatment combining low-dose radiotherapy with chemoimmunotherapy for patients with locally advanced head and neck squamous cell carcinoma (HNSCC). Participants will receive two cycles of tislelizumab, albumin-bound paclitaxel, and cisplatin, followed by radical surgery 3-4 weeks after treatment. The primary goal is to improve the pathological complete response rate while maintaining manageable side effects. This open-label, single-arm phase II trial aims to provide insights into a potentially effective neoadjuvant treatment approach.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18-70 with untreated, histologically confirmed locally advanced HNSCC eligible for radical surgery.
Not a fit: Patients with non-resectable tumors or those outside the specified age range may not benefit from this study.
Why it matters
Potential benefit: If successful, this treatment could significantly improve the response rates and outcomes for patients with advanced head and neck cancer.
How similar studies have performed: Other studies have shown promising results with similar combinations of radiotherapy and immunotherapy, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria:
1. Untreated, histologically confirmed head and neck squamous cell carcinoma (oral cavity, oropharynx, hypopharynx or larynx), staging T3-4N0M0 or T1-4N1-3M0, III-IVB, according to the eighth edition of the AJCC staging system;
2. Eligible for radical surgery, as judged by surgeons.
3. Aged ≥ 18 years and ≤ 70 years.
4. Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1.
5. Life expectancy of more than 6 months.
6. At least one measurable lesion according to RECIST 1.1.
7. Adequate organ function, based on meeting all of the following criteria (no blood components and cytologic growth factors were received within 14 days prior to the test):
1. Hemoglobin ≥ 90 g/L; absolute neutrophil count ≥ 1.5 × 109/L; and platelet count ≥ 100 × 109/L;
2. Serum albumin ≥ 28 g/L;
3. Total bilirubin ≤ 1.5 × upper limit of normal (ULN); ALT and AST ≤ 2.5 × ULN;
4. Serum creatinine ≤ 1.5 × ULN and creatinine clearance rate ≥ 50 mL/min;
5. Activated partial clotting enzyme time and international standardized ratio (INR) ≤ 1.5 × ULN (Patients on stable doses of anticoagulant therapy such as low molecular weight heparin or warfarin with INR within the expected treatment range of anticoagulants can be screened ).
43/5000
6. Thyroid Stimulating Hormone (TSH) ≤ULN; If abnormal, T3 and T4 levels should be examined, and patients with normal T3 and T4 levels can be screened.
8. Women of childbearing age should agree to the use of contraception (e.g., intrauterine devices, birth control pills, or condoms) during drug administration and for 3 months thereafter.
9. Subjects voluntarily join the study and sign an informed consent form, with good compliance.
Exclusion Criteria (Patients will be excluded if any of the following criteria is met):
1. Pregnant or lactating women.
2. A history of allergies to PD-1 inhibitors or any of albumin-bound paclitaxel or cisplatin.
3. A history of other malignant tumors within the previous 5 years or at the time of enrollment, except for cured skin basal cell carcinoma and cervical in situ cancer, as well as thyroid papilloma.
4. Uncontrolled cardiac clinical symptoms or diseases, such as :(1) NYHA class II or higher heart failure, (2) unstable angina pectoris, (3) myocardial infarction within 1 year, and (4) patients with clinically significant ventricular or ventricular arrhythmias requiring intervention.
5. Have received any of the following treatments:
1. Any research drug received prior to the first dose of the current research drug.
2. Joined another clinical study at the same time, unless it is an observational (noninterventional) clinical study or an intervention during a follow-up.
3. Needed systemic treatment with corticosteroids (more than 10 mg of prednisone or equivalent per day) or other immunosuppressants within 2 weeks prior to the first dose of the study drug, except for the use of corticosteroids for local inflammation and prevention of allergies or nausea and vomiting. In the absence of active autoimmune diseases, inhalation or partial use of steroids and adrenal corticosteroid replacements at doses greater than 10 mg per day of fentanyl equivalent is permitted.
4. Live vaccines were administered within 4 weeks prior to the first administration of research drugs.
5. Major surgery or severe trauma within four weeks of initial use of the study drug.
6. Serious infections (greater than grade 2 according to the Common Terminology Criteria for Adverse Events), such as severe pneumonia, bacteremia, and infection comorbidities, which required hospitalization, occurred within 4 weeks prior to the first dose of the study drug; baseline chest imaging examinations indicate the presence of active lung inflammation or symptoms and signs of infection within 2 weeks prior to the first dose of the study drug or indicate the need for oral or intravenous antibiotic treatment (excluding the use of preventive antibiotics).
7. A history of active autoimmune diseases and syndromes (including, but not limited to, interstitial pneumonia, colitis, hepatitis, pituitary inflammation, vasculitis, nephritis, hyperthyroidism, and hypothyroidism). Patients with vitiligo or cured childhood asthma/allergies that do not require any intervention in adulthood are not excluded.
8. A history of immunodeficiency, including HIV-positive status or other acquired congenital immunodeficiency diseases, or a history of organ transplantation and bone marrow transplantation.
9. Patients with active tuberculosis infection found by history or CT examination, or patients with active tuberculosis infection history within 1 year prior to enrollment, or patients with active tuberculosis infection history before 1 year without formal treatment.
10. Active hepatitis B (HBV DNA ≥ 2,000 IU/mL or 10,000 copies/mL) or hepatitis C (positive HCV antibody test and HCV RNA above the lower limit of detection).
11. Known history of psychotropic drug abuse, alcoholism and drug use.
12. Not suitable for inclusion, as judged by the researcher.
Where this trial is running
Zhuhai, Guangdong and 1 other locations
- Fifth Affiliated Hospital of Sun Yat-sen University — Zhuhai, Guangdong, China (Recruiting)
- Zhigang Liu — Dongguan, China (Recruiting)
Study contacts
- Study coordinator: Zhigang Liu, Dr.
- Email: liuzhg9@mail.sysu.edu.cn
- Phone: 07562526192
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.